HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1972772Generated: October 31, 2026
Formaldehyde → 5-(2-benzyl-2H-indazol-6-yl)-7-(4-(4-methylpiperazin-1-yl)phenyl]pyrrolo[2,1-f][1,2,4]triazin-4-amine
https://huagongshe.com/reaction/1972772
Participants
| Role | Name | HCID | Charge |
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| Reactant | Formaldehyde | HCID 712 | — |
| Reactant | Sodium triacetoxyborohydride | HCID 5049666 | — |
| Reactant | 5-(2-benzyl-2H-indazol-6-yl)-7-(4-piperazin-1-ylphenyl)pyrrolo[2,1-f][1,2,4]triazin-4-amine | HCID 58529498 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 5-(2-benzyl-2H-indazol-6-yl)-7-(4-(4-methylpiperazin-1-yl)phenyl]pyrrolo[2,1-f][1,2,4]triazin-4-amine | HCID 58529577 | 58% |
Reaction Steps
To a solution of 5-(2-benzyl-2H-indazol-6-yl)-7-(4-piperazin-1-ylphenyl)pyrrolo[2,1-f][1,2,4]triazin-4-amine (89 mg, 0.18 mmol) in dichloromethane (3 mL) was added formaldehyde (37% in water) (80 μL, 1.06 mmol) and sodium triacetoxyborohydride (113 mg, 0.53 mmol). The reaction was stirred (rt) for 17 h. The mixture was diluted with dichloromethane (25 mL) and was washed with H2O (1×20 mL), brine, and was dried (Na2SO4) and evaporated. The residue was purified by preparative HPLC using a gradient elution from 5% to 30% acetonitrile in water to obtain 53 mg (58%) of the desired product. 1H NMR (300 MHz, DMSO-d6) δ 8.57 (s, 1 H), 7.99-7.91 (m, 3 H), 7.86-7.79 (m, 1 H), 7.69-7.63 (m, 1 H), 7.39-7.26 (m, 5 H), 7.23-7.17 (m, 1 H), 7.06-6.98 (m, 3 H), 5.66 (s, 2 H), 3.27-3.14 (m, 4 H), 2.47-2.40 (m, 4 H), 2.22 (s, 3 H); ES-MS m/z 515.32 [M+H]+, HPLC RT (min) 2.36.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08431695B2 |
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| Source dataset | uspto-grants-2013_04 |
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| ORD ID | ord-9df24552ce504261a8cb6cc2da501b68 |
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| Source note | uspto-grants-2013_04 |
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